Evaluation of chromosomal insertion loci in the Pseudomonas putida KT2440 genome for predictable biosystems design

The development of Pseudomonas strains for industrial production of fuels and chemicals will require the integration of heterologous genes and pathways into the chromosome. Finding the most appropriate integration site to maximize strain performance is an essential part of the strain design process....

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Main Authors: Julie E. Chaves, Rosemarie Wilton, Yuqian Gao, Nathalie Munoz Munoz, Meagan C. Burnet, Zachary Schmitz, John Rowan, Leah H. Burdick, Joshua Elmore, Adam Guss, Dan Close, Jon K. Magnuson, Kristin E. Burnum-Johnson, Joshua K. Michener
Format: Article
Language:English
Published: Elsevier 2020-12-01
Series:Metabolic Engineering Communications
Online Access:http://www.sciencedirect.com/science/article/pii/S2214030120300195
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spelling doaj-70bbff40f235475ab58cc68c3bccf6b52020-11-25T03:21:33ZengElsevierMetabolic Engineering Communications2214-03012020-12-0111e00139Evaluation of chromosomal insertion loci in the Pseudomonas putida KT2440 genome for predictable biosystems designJulie E. Chaves0Rosemarie Wilton1Yuqian Gao2Nathalie Munoz Munoz3Meagan C. Burnet4Zachary Schmitz5John Rowan6Leah H. Burdick7Joshua Elmore8Adam Guss9Dan Close10Jon K. Magnuson11Kristin E. Burnum-Johnson12Joshua K. Michener13Biosciences Division, Oak Ridge National Laboratory, P.O. Box 2008, MS6342 Oak Ridge, Tennessee, 37831-6342, USAArgonne National Laboratory, USAPacific Northwest National Laboratory, USAPacific Northwest National Laboratory, USAPacific Northwest National Laboratory, USABiosciences Division, Oak Ridge National Laboratory, P.O. Box 2008, MS6342 Oak Ridge, Tennessee, 37831-6342, USABiosciences Division, Oak Ridge National Laboratory, P.O. Box 2008, MS6342 Oak Ridge, Tennessee, 37831-6342, USABiosciences Division, Oak Ridge National Laboratory, P.O. Box 2008, MS6342 Oak Ridge, Tennessee, 37831-6342, USABiosciences Division, Oak Ridge National Laboratory, P.O. Box 2008, MS6342 Oak Ridge, Tennessee, 37831-6342, USA; Pacific Northwest National Laboratory, USABiosciences Division, Oak Ridge National Laboratory, P.O. Box 2008, MS6342 Oak Ridge, Tennessee, 37831-6342, USABiosciences Division, Oak Ridge National Laboratory, P.O. Box 2008, MS6342 Oak Ridge, Tennessee, 37831-6342, USAPacific Northwest National Laboratory, USAPacific Northwest National Laboratory, USABiosciences Division, Oak Ridge National Laboratory, P.O. Box 2008, MS6342 Oak Ridge, Tennessee, 37831-6342, USA; Corresponding author.The development of Pseudomonas strains for industrial production of fuels and chemicals will require the integration of heterologous genes and pathways into the chromosome. Finding the most appropriate integration site to maximize strain performance is an essential part of the strain design process. We characterized seven chromosomal loci in Pseudomonas putida KT2440 for integration of a fluorescent protein expression construct. Insertion in five of the loci did not affect growth rate, but fluorescence varied by up to 27-fold. Three sites displaying a diversity of phenotypes with the fluorescent reporter were also chosen for the integration of a gene encoding a muconate importer. Depending on the integration locus, expression of the importer varied by approximately 3-fold and produced significant phenotypic differences. This work demonstrates the impact of the integration location on host viability, gene expression, and overall strain performance.http://www.sciencedirect.com/science/article/pii/S2214030120300195
collection DOAJ
language English
format Article
sources DOAJ
author Julie E. Chaves
Rosemarie Wilton
Yuqian Gao
Nathalie Munoz Munoz
Meagan C. Burnet
Zachary Schmitz
John Rowan
Leah H. Burdick
Joshua Elmore
Adam Guss
Dan Close
Jon K. Magnuson
Kristin E. Burnum-Johnson
Joshua K. Michener
spellingShingle Julie E. Chaves
Rosemarie Wilton
Yuqian Gao
Nathalie Munoz Munoz
Meagan C. Burnet
Zachary Schmitz
John Rowan
Leah H. Burdick
Joshua Elmore
Adam Guss
Dan Close
Jon K. Magnuson
Kristin E. Burnum-Johnson
Joshua K. Michener
Evaluation of chromosomal insertion loci in the Pseudomonas putida KT2440 genome for predictable biosystems design
Metabolic Engineering Communications
author_facet Julie E. Chaves
Rosemarie Wilton
Yuqian Gao
Nathalie Munoz Munoz
Meagan C. Burnet
Zachary Schmitz
John Rowan
Leah H. Burdick
Joshua Elmore
Adam Guss
Dan Close
Jon K. Magnuson
Kristin E. Burnum-Johnson
Joshua K. Michener
author_sort Julie E. Chaves
title Evaluation of chromosomal insertion loci in the Pseudomonas putida KT2440 genome for predictable biosystems design
title_short Evaluation of chromosomal insertion loci in the Pseudomonas putida KT2440 genome for predictable biosystems design
title_full Evaluation of chromosomal insertion loci in the Pseudomonas putida KT2440 genome for predictable biosystems design
title_fullStr Evaluation of chromosomal insertion loci in the Pseudomonas putida KT2440 genome for predictable biosystems design
title_full_unstemmed Evaluation of chromosomal insertion loci in the Pseudomonas putida KT2440 genome for predictable biosystems design
title_sort evaluation of chromosomal insertion loci in the pseudomonas putida kt2440 genome for predictable biosystems design
publisher Elsevier
series Metabolic Engineering Communications
issn 2214-0301
publishDate 2020-12-01
description The development of Pseudomonas strains for industrial production of fuels and chemicals will require the integration of heterologous genes and pathways into the chromosome. Finding the most appropriate integration site to maximize strain performance is an essential part of the strain design process. We characterized seven chromosomal loci in Pseudomonas putida KT2440 for integration of a fluorescent protein expression construct. Insertion in five of the loci did not affect growth rate, but fluorescence varied by up to 27-fold. Three sites displaying a diversity of phenotypes with the fluorescent reporter were also chosen for the integration of a gene encoding a muconate importer. Depending on the integration locus, expression of the importer varied by approximately 3-fold and produced significant phenotypic differences. This work demonstrates the impact of the integration location on host viability, gene expression, and overall strain performance.
url http://www.sciencedirect.com/science/article/pii/S2214030120300195
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